77027-53-3

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Basic information

Product Name: (2R,3R,11R,12R,20R,21R)-(+)-N,N,N',N',N,N,N',N',N,N,N',N'-dodecamethyl-1,4,7,10,13,16,19,22,25-nonaoxacycloheptacosane-2,3,11,12,20,21-hexacarboxamide
Synonyms:
CAS NO:77027-53-3
Molecular Formula:
Molecular Weight: 822.951
EINECS: N/A
Product Categories: N/A
Mol File: 77027-53-3.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,3R,11R,12R,20R,21R)-(+)-N,N,N',N',N,N,N',N',N,N,N',N'-dodecamethyl-1,4,7,10,13,16,19,22,25-nonaoxacycloheptacosane-2,3,11,12,20,21-hexacarboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,11R,12R,20R,21R)-(+)-N,N,N',N',N,N,N',N',N,N,N',N'-dodecamethyl-1,4,7,10,13,16,19,22,25-nonaoxacycloheptacosane-2,3,11,12,20,21-hexacarboxamide(77027-53-3)
EPA Substance Registry System: (2R,3R,11R,12R,20R,21R)-(+)-N,N,N',N',N,N,N',N',N,N,N',N'-dodecamethyl-1,4,7,10,13,16,19,22,25-nonaoxacycloheptacosane-2,3,11,12,20,21-hexacarboxamide(77027-53-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 77027-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 77027-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,2 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77027-53:
(7*7)+(6*7)+(5*0)+(4*2)+(3*7)+(2*5)+(1*3)=133
133 % 10 = 3
So 77027-53-3 is a valid CAS Registry Number.

77027-53-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	(2R,3R,11R,12R,20R,21R)-N2,N2,N3,N3,N11,N11,N12,N12,N20,N20,N21,N21-dodecamethyl-1,4,7,10,13,16,19,22,25-nonaoxacycloheptacosane-2,3,11,12,20,21-hexacarboxamide

1.2 Other means of identification

Product number	-
Other names	(2R,3R,11R,12R,20R,21R)-N<sup>2</sup>,N<sup>2</sup>,N<sup>3</sup>,N<sup>3</sup>,N<sup>11</sup>,N<sup>11</sup>,N<sup>12</sup>,N<sup>12</sup>,N<sup>20</sup>,N<sup>20</sup>,N<sup>21</sup>,N<sup>21</sup>-dodecamethyl-1,4,7,10,13,16,19,22,25-nonaoxacycloheptacosane-2,3,11,12,20,21-hexacarboxamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:77027-53-3 SDS

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77027-53-3Relevant articles and documents

Molecular Receptors. Functionalized and Chiral Macrocyclic Polyethers Derived from Tartaric Acid

Behr, Jean-Paul,Girodeau, Jean-Marc,Hayward, Rodney C.,Lehn, Jean-Marie,Sauvage, Jean-Pierre

, p. 2096 - 2111 (1980)

A number of functionalized and chiral macrocyclic polyethers have been synthesized by condensation of the dithallium alcoholate of (R,R)-(+)-tartaric acid derivatives with α,ω-dihalides.In this way for instance, the tetracarboxylic -O6 macrocycle 3c a

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